Back to Search Start Over

Isolation of a panel of ultra-potent human antibodies neutralizing SARS-CoV-2 and viral variants of concern.

Authors :
Gorchakov AA
Kulemzin SV
Guselnikov SV
Baranov KO
Belovezhets TN
Mechetina LV
Volkova OY
Najakshin AM
Chikaev NA
Chikaev AN
Solodkov PP
Larichev VF
Gulyaeva MA
Markhaev AG
Kononova YV
Alekseyev AY
Shestopalov AM
Yusubalieva GM
Klypa TV
Ivanov AV
Valuev-Elliston VT
Baklaushev VP
Taranin AV
Source :
Cell discovery [Cell Discov] 2021 Oct 19; Vol. 7 (1), pp. 96. Date of Electronic Publication: 2021 Oct 19.
Publication Year :
2021

Abstract

In the absence of virus-targeting small-molecule drugs approved for the treatment and prevention of COVID-19, broadening the repertoire of potent SARS-CoV-2-neutralizing antibodies represents an important area of research in response to the ongoing pandemic. Systematic analysis of such antibodies and their combinations can be particularly instrumental for identification of candidates that may prove resistant to the emerging viral escape variants. Here, we isolated a panel of 23 RBD-specific human monoclonal antibodies from the B cells of convalescent patients. A surprisingly large proportion of such antibodies displayed potent virus-neutralizing activity both in vitro and in vivo. Four of the isolated nAbs can be categorized as ultrapotent with an apparent IC <subscript>100</subscript> below 16 ng/mL. We show that individual nAbs as well as dual combinations thereof retain activity against currently circulating SARS-CoV-2 variants of concern (such as B.1.1.7, B.1.351, B.1.617, and C.37), as well as against other viral variants. When used as a prophylactics or therapeutics, these nAbs could potently suppress viral replication and prevent lung pathology in SARS-CoV-2-infected hamsters. Our data contribute to the rational development of oligoclonal therapeutic nAb cocktails mitigating the risk of SARS-CoV-2 escape.<br /> (© 2021. The Author(s).)

Details

Language :
English
ISSN :
2056-5968
Volume :
7
Issue :
1
Database :
MEDLINE
Journal :
Cell discovery
Publication Type :
Academic Journal
Accession number :
34667147
Full Text :
https://doi.org/10.1038/s41421-021-00340-8